营养盐水平对念珠藻胞外有机物产生的影响

以我国湖泊典型固氮蓝藻发状念珠藻(Nostoc flagelliforme)为研究对象,考察了氮、磷营养盐对发状念珠藻生长特性及其胞外有机物产生的影响.采用藻细胞浓度计数法表征发状念珠藻生长特性;分别采用溶解性有机碳(DOC)、三维荧光光谱(EEM)和紫外-可见光谱法,从总量和主要物质方面分析了发状念珠藻胞外有机物的产生规律.结果表明,在不同氮、磷营养水平下,发状念珠藻的4个关键生长时期基本相同,氮是控制发状念珠藻生长的关键营养控制要素;氮营养元素浓度的增高,有利于发状念珠藻产生胞外有机物,其产生量逐渐增大,而磷营养元素浓度的增高对胞外有机物产生量贡献较小,氮营养盐是发状念珠藻产生胞外有机物的关键限制因子;通过EEM谱图分析,发状念珠藻胞外有机物主要以类氨基酸类物质和类富里酸物质为主.以磷为控制营养盐时,类富里酸是主要的胞外有机物之一,以氮为控制营养盐时,类富里酸产生量极低;作为主要的胞外有机物,蛋白质和碳水化合物的产生规律显著不同,其中蛋白质含量显著高于碳水化合物含量.     

若尔盖高原湿地藻类多样性研究

分别于夏、冬两季采集若尔盖高原湿地水样,利用传统培养及显微镜检的方法和现代分子生物学方法对其藻类多样性进行了研究.结果表明,夏季水样至少培养出4种绿藻,分别为普通小球藻(Chlorella vulgaris Beij.)、浮球藻(Planktosphaeriagelatinosa G.M.Smith)、繁茂栅列藻(Scenedesmus abundans Kirchner)和柱状栅列藻(Scenedesmus bijuga Turp.),均属于绿球藻(Chlorococcales),其中普通小球藻为优势藻种,并被分离纯化.显微镜检结果表明冬季水样中主要的藻类种群为硅藻,此结果符合在低温季节天然水体中常以硅藻为主的常理.蓝藻16S rRNA基因克隆文库中的主要类群为硅藻(Bacillaripiophyta,35.3%),其次为蓝藻,包括色球藻(Chroococcales,5.9%)、念珠藻(Nostocales,11.8%)、颤藻(Oscillatoriales,11.8%)和一些未知种属的蓝藻类群(Unclassified Cyanobacteria,35.3%),还发现一些与低温环境微生物相关的类群,如颤藻目细纤菌属(Leptolyngbya).     

祁连山高山草甸土壤CO2通量的时空变化及其影响分析

采用Li-6400便携式光合作用测量系统连接Li-6400-09土壤呼吸室,在2004年生长季节对祁连山高山草甸土壤CO₂通量沿海拔梯度进行了野外定位试验,统计分析了水热因子及根系生物量对高山草甸土壤CO₂通量特征的可能影响.结果表明,土壤CO₂通量存在明显的空间变化规律, 沿海拔梯度土壤CO₂通量随着海拔梯度的增加而逐渐减小,其变异系数逐渐增加;就日变化而言,土壤CO₂通量晚间维持在较低水平,02：00～06：00最低,在07：00～08：30开始升高,11：00～16：00达到峰值,16：00～18：30开始下降,整个过程呈单峰曲线.土壤CO₂通量的日平均值介于(0.56±0.32) ～ (2.53±0.76) μmol·(m²·s)^-1.从季节变化来看,土壤CO₂通量均以夏秋季较高,春冬季排放量较低,7～8月份达到最大值［4.736 μmol·(m²·s)^-1］,6月与9月份次之,5月与10月份基本一致,整个生长过程总的变化趋势呈单峰曲线形式.高山草甸土壤CO₂通量在植物生长季与10 cm土壤温度、土壤含水量、根系生物量都存在不同程度的正相关关系,表明高山草甸土壤CO₂通量的空间变异主要受温度、水分和植物根系的综合影响.     

Alga-lysing bioreactor and dominant bacteria strain

Alga-lysing bacteria have been paid much attention to in recent years. In this study, the alga-lysing strain P05 which was isolated from an immobilizing biosystem was immobilized by coke and elastic filler, forming two biological reactors. The removal efficiencies of algae, NH4^＋-N and organic matter using the two reactors were studied. The results showed that strain P05 was an ideal algal-lysing bacteria strain because it was easy to be immobilized by coke and elastic filler which are of cheap, low biodegradability and the simple immobilization procedure. After 7 d filming, the biological film could be formed and the reactors were used to treat the eutrophic water. These two reactors were of stability and high effect with low cost and easy operation. The optimal hydraulic retention time （HRT） of each reactor was 4 h. The algae removal rates were 80.38% and 82.1% （in term of Chl-α） of coke reactor and filler reactor, respectively. And that of NH4^＋-N were 52.3% and 52.7%. The removal rates of CODMn were 39.03% and 39.64%. The strain P05 was identified as Bacillus sp. by PCR amplification of the 16S rRNA gene, BLAST analysis, and comparison with sequences in the GenBank nucleotide database.     

Resistance and biosorption mechanism of silver ions by Bacillus cereus biomass

Biosorption of silver ions onto Bacillus cereus biomass was investigated. Overall kinetic experiments were performed for the determination of the necessary contact time for the attainment of equilibrium. It was found that the overall biosorption process was best described by pseudo second-order kinetic model. The crystals detected by scanning electron microscope and X-ray photoelectron spectroscopy suggested the precipitation was a possible mechanism of biosorption. The molecular genetics of silver resistance of B. cereus biomass was also detected and illustrated by a whole cell sensor tool.     

Chemical cleaning of fouled PVC membrane during ultrafiltration of algal-rich water

Cleaning of hollow-fibre polyvinyl chloride (PVC) membrane with di erent chemical reagents after ultrafiltration of algal-rich water was investigated. Among the tested cleaning reagents (NaOH, HCl, EDTA, and NaClO), 100 mg/L NaClO exhibited the best performance (88.4% 1.1%) in removing the irreversible fouling resistance. This might be attributed to the fact that NaClO could eliminate almost all the major foulants such as carbohydrate-like and protein-like materials on the membrane surface, as confirmed by Fourier transform infrared spectroscopy analysis. However, negligible irreversible resistance (1.5% 1.0%) was obtained when the membrane was cleaning by 500 mg/L NaOH for 1.0 hr, although the NaOH solution could also desorb a portion of the major foulants from the fouled PVC membrane. Scanning electronic microscopy and atomic force microscopy analyses demonstrated that 500 mg/L NaOH could change the structure of the residual foulants on the membrane, making them more tightly attached to the membrane surface. This phenomenon might be responsible for the negligible membrane permeability restoration after NaOH cleaning. On the other hand, the microscopic analyses reflected that NaClO could e ectively remove the foulants accumulated on the membrane surface.     

刘家峡水库水环境质量生物学评价研究

2008年黄河丰水期和2009年黄河枯水期,对研究区6处标志性区域进行随机采样,采用活体观察和固定染色法鉴定藻类种类,直接计数法统计藻类数量,共鉴定到藻类114种(包括22个未定名物种),隶属于9门11纲17目34科55属。其中,硅藻门47种,占41.22%,以无壳缝目为优势类群;绿藻门24种,占21.05%,为次优势类群;蓝藻门,金藻门,裸藻门为常见类群;隐藻门、甲藻门和黄藻门均为罕见类群。利用藻类群落结构特征、优势种类、藻类污染指数和污生指数等指标对刘家峡水库水质进行评价,结果表明:刘家峡水库水质在1#、2#样区较清洁,3#、4#样区为轻-中度污染,5#、6#样区为重度污染,与采用粪大肠肝菌、DO指标评价结果具有良好一致性。     

星肋小环藻、铜绿微囊藻春化作用基因控制机理

实验证实了星肋小环藻、铜绿微囊藻的春化作用后,其暴发控制机理成为研究重点。该文通过分析单细胞生物基因操作原理、遗传物质转录复制控制、温度对蛋白质的作用和酶原激活过程等,研究微藻春化作用基因控制机理,提出基因控制模型:激活基因-操纵基因连锁的基因操纵模型,由基因操纵子、调节基因和激活基因组成。该模型阐释2种藻类春末夏初大规模暴发机理:春季,调节基因产生的调节蛋白原被调节蛋白激活酶激活产生的调节蛋白与操纵基因结合,启动结构基因转录合成DNA合成酶系,DNA复制完成,藻体裂殖(繁殖)群体增长;夏季,高温下温度敏感的调节蛋白激活酶变性,使调节蛋白原激活产生变构的调节蛋白,同时与操纵基因和激活基因结合,激活基因不能产生调节蛋白激活酶激活调节蛋白原产生激活蛋白,这时铜绿微囊藻进入生长被抑制状态,星肋小环藻进入高温休眠状态;进入秋季,因之前无低温出现使热变性的激活酶复性,激活产生正常的调节蛋白与操纵基因结合,启动结构基因复制繁殖所需DNA酶系,尽管秋季温光适宜,星肋小环藻不会生长活动,铜绿微囊藻可生长但生长速度低于春末夏初时的生长速度;进入冬季,低温使热变性的激活酶复性,等待来年春暖激活调节蛋白原,启动新一年的藻生长。     

不同浓度Cd~(2+)对酿酒酵母的毒害作用研究

以"模式生物"——酿酒酵母(Saccharomyces cerevisiae)为载体,通过测定酵母细胞的生物量、活细胞/死细胞的计数比值以及胞外聚合物(EPS)的含量,研究了不同浓度的Cd2+(Cd2+浓度分别为0.0mg/L、0.1mg/L、0.5mg/L、1.0mg/L、2.0mg/L、8.0mg/L)对酿酒酵母的毒害作用。试验结果表明:当Cd2+浓度小于或等于0.1mg/L时,活细胞/死细胞的计数比值随着时间的推移分别降低了7.86和8.37,在0.5 mg/L、1.0 mg/L和2.0mg/L的Cd2+浓度下,活细胞/死细胞的计数比值则分别上升了3.35、5.64和0.89,8.0mg/L浓度的Cd2+则会完全抑制酵母细胞的增殖,活细胞/死细胞的计数比值波动在0.86~1.11之间;同时,随着Cd2+浓度的上升,酵母细胞的生物量会逐渐减少,0.1mg/L浓度的Cd2+对酵母细胞生物量无明显影响,0.5~8.0mg/L浓度的Cd2+可使酵母细胞生物量比不含Cd2+的培养基分别下降了7.01%、35.14%、59.89%和96.86%;此外,0.5 mg/L和1.0mg/L浓度的Cd2+能显著刺激酵母细胞分泌更多的EPS,增幅分别为20.26%和7.54%。上述结果表明酵母细胞在一定的Cd2+浓度下可以通过提高EPS的产量来抵御Cd2+对细胞的毒性作用。     

藻类水体Cd2+毒性快速监测新方法研究

采用藻类生长抑制试验和光合活性抑制试验两种方法对蛋白核小球藻受不同浓度Cd2+胁迫作用下叶绿素浓度及藻活性荧光参数进行测量,依据Sigmoidal曲线拟合及单因素方差分析(one-way ANOVA)的方法对Cd2+不同胁迫时间下藻活性抑制率和96 h比生长率抑制率的相关性进行研究.结果表明,48、53、72、77和96 h的藻活性抑制率和96 h比生长率抑制率间具有较好的S函数关系(R2>0.95),因此可采用藻活性抑制率48 h-EC10和53 h-EC10来代替96 h的藻类半数比生长率抑制率EC50进行Cd2+藻类毒性实验评价.进一步分析了蛋白核小球藻受Cd2+胁迫48 h和53 h藻活性抑制率和Cd2+毒性当量的剂量-效应关系.该方法为实验室内单一Cd2+毒性的监测提供了一种快速有效的新方法,为水环境综合毒性预警提供了一种切实可行的方法依据.